Page 289 - Origin and Prediction of Abnormal Formation Pressures
P. 289

260                                  H.H. RIEKE, G.V. CHILINGAR AND J.O. ROBERTSON JR.
                         A  (cations)                        B  (anions)

                 F  HC03CI  S02 I                    K +  Ca 2+ Mg2+Na§
                  50  .00  950016d00                  I00  '00  ~00   ~k   '   "   ,
                                                                 -\
             E                                                   -  \    /
             C~                                                              Na+   i
             c)
              m.
            m      O0  300  9000
             12)                                      300 ~00 700
             E

             C:
             0                          \
            m~,,
             0                 ,     co3- \
             Imm                                                        9    ~/,  "
             C:   50  20C  1850(                      200  500 600
             0
             0                 9              I:
             r"
             0                /             \
                               .....  W- .....  ..',,,t#
                                     .
                                                                          ,     ,  I
                  wO  -10C  "1800   I   ,    t   ~..   "10C  "40C  "500
                             0     20    40     (~0                   20    40     60
                            Amount     of  Extruded  Solution,  cm      3

            Fig.  10-17.  Variations  in  the  concentration  of dissolved  constituents  with  increasing  compaction pressure  in
            the subsequent fractions of expelled solutions from smectite clay hydrated in seawater:  (A) anions; (B) cations.
            (Modified after Chilingarian  et al.,  1973, figs.  1 and 2, p. 396.  In Chilingarian  et al.,  1994,  fig. 5-12, p.  131.)


            or  at  least  remain  constant,  before  starting  to  decrease  with  increasing  overburden
            pressure.
               Chilingar  and  Rieke  (1976)  saturated  a  sample  consisting  of 50%  smectite  and  50%
            illite in seawater, having a salinity of 34,500 mg/1, for ten days. After shaking vigorously
            the sample several times a day, the supernatant  liquid (leachate) was removed,  analyzed,
            and found to have a total dissolved  solids content of 37,900  mg/1.  The higher salinity of
            the  supernatant  water as  compared  to  the  initial  seawater salinity  is possibly  due  to the
            presence of soluble salts in the original sample. The authors assumed that the supernatant
            liquid had the same composition  as the free pore  water. The remaining  saturated sample
            was placed in a hydrostatic  compaction  cell, squeezed and the successive portions  of the
            expelled  water  were  analyzed.  Fig.  10-18  shows  the  concentrations  of Ca 2+ and Mg 2+,
            whereas the concentrations  of C1-  and total dissolved  solids are presented in Figs.  10-19
            and  20,  respectively.  These  results  indicate  that  the  total  concentration  of  expelled
            solutions  goes through  a maximum before  starting to decrease  with increasing pressure.
            The  concentrations  of Ca 2+  and  Mg 2+  ions  in  squeezed-out  solutions,  however,  start to
            increase  again during  the  latest stages  of compaction.  This  can possibly  be attributed to
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